A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17377873



Internal ID22435743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:34834947..34837580hg38UCSC Ensembl
chr14:35304153..35306786hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg382634
hg192634
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5928798
Supporting Variants
Samples
Known GenesBAZ1A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17377873
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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